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3-O-Descladinosyl-3-keto-6-O-methylerythromycin A E-9-O-[3-(3'-quinolyl)-2-propyl]oxime 11,12-cyclic carbonate ID: ALA2316684
PubChem CID: 71571086
Max Phase: Preclinical
Molecular Formula: C43H63N3O11
Molecular Weight: 797.99
Molecule Type: Small molecule
This compound is available for customization.
Associated Items:
Names and Identifiers Canonical SMILES: CC[C@H]1OC(=O)[C@H](C)C(=O)[C@H](C)[C@@H](O[C@@H]2O[C@H](C)C[C@H](N(C)C)[C@H]2O)[C@](C)(OC)C[C@@H](C)/C(=N\OCCCc2cnc3ccccc3c2)[C@H](C)[C@H]2OC(=O)O[C@@]21C
Standard InChI: InChI=1S/C43H63N3O11/c1-12-33-43(8)38(56-41(50)57-43)26(4)34(45-52-19-15-16-29-21-30-17-13-14-18-31(30)44-23-29)24(2)22-42(7,51-11)37(27(5)35(47)28(6)39(49)54-33)55-40-36(48)32(46(9)10)20-25(3)53-40/h13-14,17-18,21,23-28,32-33,36-38,40,48H,12,15-16,19-20,22H2,1-11H3/b45-34+/t24-,25-,26+,27+,28-,32+,33-,36-,37-,38-,40+,42-,43-/m1/s1
Standard InChI Key: FHODXLUICIGDBI-AKLJTMLOSA-N
Molfile:
RDKit 2D
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M END Associated Targets(non-human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: NoChirality: NoAvailability: NoProdrug: No
Drug Indications MESH ID MESH Heading EFO IDs EFO Terms Max Phase for Indication References
Mechanisms of Action Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References
Calculated Properties Molecular Weight: 797.99Molecular Weight (Monoisotopic): 797.4463AlogP: 5.89#Rotatable Bonds: 10Polar Surface Area: 164.54Molecular Species: NEUTRALHBA: 14HBD: 1#RO5 Violations: 3HBA (Lipinski): 14HBD (Lipinski): 1#RO5 Violations (Lipinski): 3CX Acidic pKa: 8.93CX Basic pKa: 8.27CX LogP: 7.15CX LogD: 6.54Aromatic Rings: 2Heavy Atoms: 57QED Weighted: 0.13Np Likeness Score: 0.94
References 1. Liang JH, An K, Lv W, Cushman M, Wang H, Xu YC.. (2013) Synthesis, antibacterial activity and docking of 14-membered 9-O-(3-arylalkyl) oxime 11,12-cyclic carbonate ketolides., 59 [PMID:23202851 ] [10.1016/j.ejmech.2012.10.054 ]